Built on four non-negotiable safety pillars.
In an industry where 70%+ of supplements fail independent label-claim testing, NervEase Lab holds itself to a different standard.
Made in the U.S.A.
Manufactured exclusively in the United States. Faster batch traceability, U.S. FDA jurisdiction, U.S. labor and environmental standards.
FDA-Registered Facility
Our manufacturing partner is registered with the U.S. FDA under 21 CFR Part 111 (Dietary Supplement cGMP). Subject to FDA inspection.
cGMP Certified
Independent third-party audited current Good Manufacturing Practice. Identity testing, potency testing, batch records, full traceability.
Third-Party Lab Tested
Every batch tested by an ISO 17025-accredited laboratory for identity, potency, heavy metals, microbiology, and pesticide residues.
Test Standards
| Test | Standard | Why It Matters |
|---|---|---|
| Active potency | ±10% of label claim | You get what's on the label |
| Heavy metals | Below USP <232> | Lead, cadmium, mercury, arsenic safe |
| Microbiology | Below USP <2021> | E. coli, Salmonella, yeast, mold screened |
| Pesticide residues | EPA tolerance limits | Clean botanical sourcing |
| Identity (HPTLC/HPLC) | Pharmacopeial monographs | Each plant is genuinely what it claims |
Reporting an Adverse Event
If you experience a reaction you believe may be related to NervEase, contact us within 24 hours at safety@nerveaselab.com or call 1-855-637-8327. We also encourage reporting serious adverse events to FDA MedWatch at fda.gov/safety/medwatch.